Search research articles
Contact Us
Filters
Showing results (1-10 of 4) with videos related to
Page
of 1
Sort By:
Journal of Clinical Pathology
|
May 13, 1998
Development of a multiplex ARMS test for mutations in the HFE gene associated with hereditary haemochromatosis
D Baty, A Terron Kwiatkowski, D Mechan, et al.
The British Journal of Dermatology
|
June 25, 2004
Atypical epidermolytic palmoplantar keratoderma presentation associated with a mutation in the keratin 1 gene
A Terron-Kwiatkowski, A Terrinoni, B Didona, et al.
Allergy
|
March 1, 2008
Filaggrin null mutations are associated with increased asthma exacerbations in children and young adults
K Basu, C N A Palmer, B J Lipworth, et al.
The British Journal of Dermatology
|
March 18, 2014
Under-recognition of acral peeling skin syndrome: 59 new cases with 15 novel mutations
W Szczecinska, D Nesteruk, K Wertheim-Tysarowska, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 4) with videos related to
Sort By:
Page
of 1
Journal of Clinical Pathology
|
May 13, 1998
Development of a multiplex ARMS test for mutations in the HFE gene associated with hereditary haemochromatosis
D Baty, A Terron Kwiatkowski, D Mechan, et al.
The British Journal of Dermatology
|
June 25, 2004
Atypical epidermolytic palmoplantar keratoderma presentation associated with a mutation in the keratin 1 gene
A Terron-Kwiatkowski, A Terrinoni, B Didona, et al.
Allergy
|
March 1, 2008
Filaggrin null mutations are associated with increased asthma exacerbations in children and young adults
K Basu, C N A Palmer, B J Lipworth, et al.
The British Journal of Dermatology
|
March 18, 2014
Under-recognition of acral peeling skin syndrome: 59 new cases with 15 novel mutations
W Szczecinska, D Nesteruk, K Wertheim-Tysarowska, et al.
Page
of 1